Tom Van Agtmael

Summary

Affiliation: National Institute for Medical Research
Country: UK

Publications

  1. ncbi request reprint Parametric and non-parametric linkage analysis of several candidate regions for genes for human handedness
    Tom Van Agtmael
    Murdoch Childrens Research Institute, Royal Children s Hospital, Parkville, Melbourne, Australia
    Eur J Hum Genet 10:623-30. 2002
  2. ncbi request reprint Parametric and nonparametric genome scan analyses for human handedness
    Tom Van Agtmael
    Murdoch Childrens Research Institute, Royal Children s Hospital, Melbourne, Australia
    Eur J Hum Genet 11:779-83. 2003
  3. ncbi request reprint 17th International Mouse Genome Conference
    Ian Smyth
    MRC Human Genetics Unit, Western General Hospital, Crewe Rd, Edinburgh, EH4 2XU United Kingdom
    Mamm Genome 15:509-14. 2004
  4. ncbi request reprint Dominant mutations of Col4a1 result in basement membrane defects which lead to anterior segment dysgenesis and glomerulopathy
    Tom Van Agtmael
    Molecular Physiology, Centre for Cardiovascular Science, University of Edinburgh, UK
    Hum Mol Genet 14:3161-8. 2005
  5. ncbi request reprint COL4A1 mutations and hereditary angiopathy, nephropathy, aneurysms, and muscle cramps
    Emmanuelle Plaisier
    INSERM Unité 702, Universite Pierre et Marie Curie, Paris 6, Unités Mixtes de Recherche Scientifique 702, Assistance Publique Hopitaux de Paris, Hopital Tenon, France
    N Engl J Med 357:2687-95. 2007

Collaborators

  • Ian J Jackson
  • Emmanuelle Plaisier
  • Ian Smyth
  • Beatrice Mougenot
  • Michel Fardeau
  • Sonia Alamowitch
  • Michel Dracon
  • Etienne Roullet
  • Pierre Ronco
  • Olivier Gribouval
  • Corinne Antignac
  • Marie Christine Verpont
  • Dontscho Kerjaschki
  • Salomon Yves Cohen
  • Beatrice Marro
  • Thomas Desmettre
  • Catherine Prost

Detail Information

Publications5

  1. ncbi request reprint Parametric and non-parametric linkage analysis of several candidate regions for genes for human handedness
    Tom Van Agtmael
    Murdoch Childrens Research Institute, Royal Children s Hospital, Parkville, Melbourne, Australia
    Eur J Hum Genet 10:623-30. 2002
    ..This demonstrates the power to identify the genes specifying handedness by the conduct of extended genetic studies on these and similar cohorts...
  2. ncbi request reprint Parametric and nonparametric genome scan analyses for human handedness
    Tom Van Agtmael
    Murdoch Childrens Research Institute, Royal Children s Hospital, Melbourne, Australia
    Eur J Hum Genet 11:779-83. 2003
    ..These results suggest that handedness is a human quantitative trait locus and that the proposed non-Mendelian monogenic models are incorrect...
  3. ncbi request reprint 17th International Mouse Genome Conference
    Ian Smyth
    MRC Human Genetics Unit, Western General Hospital, Crewe Rd, Edinburgh, EH4 2XU United Kingdom
    Mamm Genome 15:509-14. 2004
  4. ncbi request reprint Dominant mutations of Col4a1 result in basement membrane defects which lead to anterior segment dysgenesis and glomerulopathy
    Tom Van Agtmael
    Molecular Physiology, Centre for Cardiovascular Science, University of Edinburgh, UK
    Hum Mol Genet 14:3161-8. 2005
    ....
  5. ncbi request reprint COL4A1 mutations and hereditary angiopathy, nephropathy, aneurysms, and muscle cramps
    Emmanuelle Plaisier
    INSERM Unité 702, Universite Pierre et Marie Curie, Paris 6, Unités Mixtes de Recherche Scientifique 702, Assistance Publique Hopitaux de Paris, Hopital Tenon, France
    N Engl J Med 357:2687-95. 2007
    ..However, the causative genes for a number of hereditary multicystic kidney diseases, myopathies with cramps, and heritable intracranial aneurysms remain unknown...